Downregulated LncRNA-ANCR promotes osteoblast differentiation by targeting EZH2 and regulating Runx2 expression

被引:230
|
作者
Zhu, Lin [1 ]
Xu, Pei-Cheng [1 ]
机构
[1] Dent Clin Xuhui Dist, Dept Oral Med, Shanghai 200032, Peoples R China
关键词
ANCR; EZH2; Runx2; Osteoblast differentiation; LONG NONCODING RNAS; EMBRYONIC STEM-CELLS; OSTEOGENIC DIFFERENTIATION; TRANSCRIPTION FACTORS; SKELETAL-MUSCLE; FUNCTIONAL-ROLE; PLURIPOTENCY; METHYLATION; REQUIRES;
D O I
10.1016/j.bbrc.2013.02.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Long noncoding RNAs (IncRNAs) are key regulators of diverse biological processes such as transcriptional regulation, cell growth and differentiation. Previous studies have demonstrated that the.1ncRNA-ANCR (anti-differentiation ncRNA) is required to maintain the undifferentiated cell state within the epidermis. However, little is known about whether ANCR regulates osteoblast differentiation. In this study, we found that the ANCR expression level is significantly decreased during hFOB1.19 cell differentiation. ANCR-siR-NA blocks the expression of endogenous ANCR, resulting in osteoblast differentiation, whereas ANCR overexpression is sufficient to inhibit osteoblast differentiation. We further demonstrated that ANCR is associated with enhancer of zeste homolog 2 (EZH2) and that this association results in the inhibition of both Runx2 expression and subsequent osteoblast differentiation. These data suggest that ANCR is an essential mediator of osteoblast differentiation, thus offering a new target for the development of therapeutic agents to treat bone diseases. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:612 / 617
页数:6
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